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Anticonvulsants before 1993
Generic
(Brand name)
Abbreviation |
Oral Formulations
Usual adult dose
(Therapeutic level if available) |
Quick notes |
Carbamazepine
(Tegretol, Tegretol XR )
CBZ |
 | Susp: 100mg/5ml |
 | Chewable tab: 100 mg |
 | Tab: 200 mg |
 | Teg XR: 100, 200, 400 mg |
 | Dose: 400-1600 mg/day, bid to qid. |
|
T 1/2: 11-24 hr
Prot binding: 75%
Metabolism: hepatic
Mechanism: Na channel blocker
Therapeutic range: 4-12 ug/ml |
| Carbamazepine (Carbatrol) |
 | Cap: 200, 300mg, may open & sprinkle |
 | Dose: 400-1600 mg/day bid to qid. |
|
| Clonazepam (Klonopin) CZP |
 | Tab: 0.5, 1, 2 mg |
 | Dose: 0.5 mg tid, up to 20 mg/day |
|
T 1/2: 18-50 hours
Metabolism: hepatic
Tolerance to antiepileptic effect may develop up to 30% of patients. |
| Ethosuximide (Zarontin) ESM |
 | Capsule: 250 mg |
 | Solution: 250 mg/5 ml |
 | Dose: start 250 mg bid, up to 1500 mg/d |
|
T 1/2 adult: 50-60 hour
Metabolism: 20% excreted renal, 65% hepatic. |
Phenobarbital
PHB |
 | Susp: 20mg/5ml, Tab: 15, 30, 60,100mg |
 | Dose: 30-180 mg/day
(level: 10-40 ug/ml) |
|
T 1/2: 96 hr
Prot binding: 40%
Metabolism: hepatic
Mechanism: GABA receptor agonist |
Phenytoin (Dilantin)
PHT |
Susp: 125mg/5ml, Cap: 30, 100mg
Dose: 200-500 mg/day qd to bid
(level: 10-20 ug/ml) |
T 1/2: 22 hr
Prot binding: 90%
Metabolism: hepatic
Mechanism: Na channel blocker |
Primidone (Mysoline)
|
Susp: 250mg/5ml, Tablet: 50,250mg
Dose: 250-1500mg/day bid to tid
(level: Primidone 5-13 ug/ml, Phenobarb 10-40ug / ml) |
T 1/2: 6-8 hr
Prot binding: 70%
Metabolism: hepatic to PEMA & phenobarbital
Mechanism: GABA receptor agonist |
Valproic acid (Depakene, Dapakote)
VPA |
Susp: 250mg/5ml, Tab: 125, 250, 500mg, Sprinkle cap: 125 mg
Dose: 375-3000 mg/day, given bid to tid
(level: 50-100 ug/ml) |
T 1/2: 8-16 hr
Prot binding: 90%
Metabolism: hepatic
Mechanism: Na channel blocker |
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* Approximate
** Active metabolite Phenobarbital has half life of 96 hours

Side effects
of Anticonvulsants
| Medication |
Common side effect
(usually dose dependent) |
Uncommon but serious side effect,
idiosyncratic |
| Carbamazepine |
Drowsiness, ataxia, leukopenia |
Rash, hyponatremia, aplastic anemia, hepatitis,
pancreatitis |
| Felbamate |
Insomnia, weight loss, headache, decreased appetite |
Aplastic anemia: present average 154 days after
therapy, risk: 1:4000 to 5000
Risk of fatal hepatotoxic effect 1:26,000 to 34,000 |
| Gabapentin |
drowsiness, fatigue, dizziness and possible movement
disorder |
none recognized |
| Gabatril |
dizzy, nervous, tremor, abdominal pain |
none recognized |
| Lamotrigine |
Rash (up to 10%, may be related to fast titration),
drowsiness, nausea |
none recognized |
Phenobarbital
Primidone |
Hyperactivity in children, drowsiness, slowing of cognitive
functions, ataxia |
Rash, Stevens-Johnson syn, depression |
| Phenytoin |
drowsiness, nystagmus, ataxia, gingival hypertrophy |
Rash, hepatitis, hirsutism, peripheral neuropathy? |
| Topiramate |
tiredness, dizzy, ataxia, drowsy, nervous, psychomotor
slowing |
kidney stone, 1.5% |
| Valproic acid |
tremor, thrombo-cytopenia, weight gain |
hair loss, hepatitis, pancreatitis |
Carbamazepine
 | Drugs that inhibit CYP 3A4 and increase Carbamazepine level
 | More common ones: Cimetidine, diltiazem, fluoxetine, macrolides, erythromycin,
nicotinamide, propoxyphene, ketaconazole, verapamil, valproate |
|
 | Drugs that induce CYP3A4 and reduce Carbamazepine level
 | Felbamate, Rifampin, phenobarbital, Phenytoin, Primidone, Primidone, Theophylline |
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Further reading
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